Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion description "[We propose that familial cortical myoclonus is a novel movement disorder that may be caused by mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion evidence source_evidence_literature NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion SIO_000772 22926851 NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion wasDerivedFrom befree-20140225 NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion wasGeneratedBy ECO_0000203 NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.